| Year |
Citation |
Score |
| 2020 |
He F, Flores BN, Krans A, Frazer M, Natla S, Niraula S, Adefioye O, Barmada SJ, Todd PK. The carboxyl termini of RAN translated GGGGCC nucleotide repeat expansions modulate toxicity in models of ALS/FTD. Acta Neuropathologica Communications. 8: 122. PMID 32753055 DOI: 10.1186/S40478-020-01002-8 |
0.593 |
|
| 2019 |
Linsalata AE, He F, Malik AM, Glineburg MR, Green KM, Natla S, Flores BN, Krans A, Archbold HC, Fedak SJ, Barmada SJ, Todd PK. DDX3X and specific initiation factors modulate FMR1 repeat-associated non-AUG-initiated translation. Embo Reports. e47498. PMID 31347257 DOI: 10.15252/Embr.201847498 |
0.628 |
|
| 2017 |
Sellier C, Buijsen RA, He F, Natla S, Jung L, Tropel P, Gaucherot A, Jacobs H, Meziane H, Vincent A, Champy MF, Sorg T, Pavlovic G, Wattenhofer-Donze M, Birling MC, et al. Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome. Neuron. PMID 28065649 DOI: 10.1016/J.Neuron.2016.12.016 |
0.651 |
|
| 2016 |
Yang WY, He F, Strack RL, Oh SY, Frazer M, Jaffrey SR, Todd PK, Disney MD. Small Molecule Recognition and Tools to Study Modulation of r(CGG)exp in Fragile X-Associated Tremor Ataxia Syndrome. Acs Chemical Biology. PMID 27276216 DOI: 10.1021/Acschembio.6B00147 |
0.61 |
|
| 2016 |
He F, Jones JM, Figueroa-Romero C, Zhang D, Feldman EL, Goutman SA, Meisler MH, Callaghan BC, Todd PK. Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci. Neurology. Genetics. 2: e71. PMID 27274540 DOI: 10.1212/Nxg.0000000000000071 |
0.481 |
|
| 2015 |
Oh SY, He F, Krans A, Frazer M, Taylor JP, Paulson HL, Todd PK. RAN translation at CGG repeats induces ubiquitin proteasome system impairment in models of fragile X-associated tremor ataxia syndrome. Human Molecular Genetics. 24: 4317-26. PMID 25954027 DOI: 10.1093/Hmg/Ddv165 |
0.719 |
|
| 2015 |
He F, James A, Raje H, Ghaffari H, DiMario P. Deletion of Drosophila Nopp140 induces subcellular ribosomopathies. Chromosoma. 124: 191-208. PMID 25384888 DOI: 10.1007/S00412-014-0490-9 |
0.431 |
|
| 2014 |
He F, Krans A, Freibaum BD, Taylor JP, Todd PK. TDP-43 suppresses CGG repeat-induced neurotoxicity through interactions with HnRNP A2/B1. Human Molecular Genetics. 23: 5036-51. PMID 24920338 DOI: 10.1093/Hmg/Ddu216 |
0.639 |
|
| 2013 |
Todd PK, Oh SY, Krans A, He F, Sellier C, Frazer M, Renoux AJ, Chen KC, Scaglione KM, Basrur V, Elenitoba-Johnson K, Vonsattel JP, Louis ED, Sutton MA, Taylor JP, et al. CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome. Neuron. 78: 440-55. PMID 23602499 DOI: 10.1016/J.Neuron.2013.03.026 |
0.728 |
|
| 2013 |
Meisler MH, Grant AE, Jones JM, Lenk GM, He F, Todd PK, Kamali M, Albin RL, Lieberman AP, Langenecker SA, McInnis MG. C9ORF72 expansion in a family with bipolar disorder. Bipolar Disorders. 15: 326-32. PMID 23551834 DOI: 10.1111/Bdi.12063 |
0.494 |
|
| 2013 |
Sellier C, Freyermuth F, Tabet R, Tran T, He F, Ruffenach F, Alunni V, Moine H, Thibault C, Page A, Tassone F, Willemsen R, Disney MD, Hagerman PJ, Todd PK, et al. Sequestration of DROSHA and DGCR8 by expanded CGG RNA repeats alters microRNA processing in fragile X-associated tremor/ataxia syndrome. Cell Reports. 3: 869-80. PMID 23478018 DOI: 10.1016/J.Celrep.2013.02.004 |
0.62 |
|
| 2012 |
Zhang D, Iyer LM, He F, Aravind L. Discovery of Novel DENN Proteins: Implications for the Evolution of Eukaryotic Intracellular Membrane Structures and Human Disease. Frontiers in Genetics. 3: 283. PMID 23248642 DOI: 10.3389/Fgene.2012.00283 |
0.373 |
|
| 2011 |
He F, Todd PK. Epigenetics in nucleotide repeat expansion disorders. Seminars in Neurology. 31: 470-83. PMID 22266885 DOI: 10.1055/S-0031-1299786 |
0.497 |
|
| 2008 |
He F, Doucet JA, Stephens JM. Caspase-mediated degradation of PPARgamma proteins in adipocytes. Obesity (Silver Spring, Md.). 16: 1735-41. PMID 18497737 DOI: 10.1038/Oby.2008.269 |
0.34 |
|
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